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Biotechnology Project Manager Jobs in Riverside, CA

Project Engineer II to III

Irvine, CA · On-site

$90K - $110K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... biotech manufacturing clients. In this role, you will quickly learn common client practices ... management and cGxP best practices to drive your overall success. Projects range from design ...

Project Engineer II to III

Irvine, CA · On-site

$90K - $110K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... biotech manufacturing clients. In this role, you will quickly learn common client practices ... management and cGxP best practices to drive your overall success. Projects range from design ...

Project Engineer II to III

Irvine, CA · On-site

$90K - $110K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... biotech manufacturing clients. In this role, you will quickly learn common client practices ... management and cGxP best practices to drive your overall success. Projects range from design ...

Project Engineer

Jurupa Valley, CA · On-site

$81.10 - $110/hr

  • Retirement

  • PTO

Time management** -- Ability to prioritize tasks and manage multiple projects.**Interpersonal ... Among the industries served are the chemical processing, biotechnology, pharmaceutical, oil & gas ...

New

Project Engineer

Jurupa Valley, CA · On-site

$81K - $110K/yr

  • Retirement

  • PTO

Time management - Ability to prioritize tasks and manage multiple projects. Interpersonal Skills ... Among the industries served are the chemical processing, biotechnology, pharmaceutical, oil & gas ...

Project Engineer

Jurupa Valley, CA · Hybrid

$81K - $110K/yr

  • Retirement

  • PTO

Time management - Ability to prioritize tasks and manage multiple projects. Interpersonal Skills ... Among the industries served are the chemical processing, biotechnology, pharmaceutical, oil & gas ...

Engineering Manager

Grand Terrace, CA · On-site

$138K - $152K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Ensures new product development projects are successfully completed on time * Ensures product ... Biotech, Quantex™, Quattroflow ® , and Wilden ® . PSG products are manufactured on three ...

Engineering Manager

Grand Terrace, CA · On-site

$138K - $152K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Ensures new product development projects are successfully completed on time * Ensures product ... Biotech, Quantex™, Quattroflow ® , and Wilden ® . PSG products are manufactured on three ...

Engineering Manager

Grand Terrace, CA

$138K - $152K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Ensures new product development projects are successfully completed on time * Ensures product ... Biotech, Quantex™, Quattroflow ® , and Wilden ® . PSG products are manufactured on three ...

Engineering Manager

Grand Terrace, CA · On-site

$138K - $152K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Ensures new product development projects are successfully completed on time * Ensures product ... Biotech, Quantex™, Quattroflow ® , and Wilden ® . PSG products are manufactured on three ...

Engineering Manager

Grand Terrace, CA

$138K - $152K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Ensures new product development projects are successfully completed on time * Ensures product ... Biotech, Quantex, Quattroflow, and Wilden. PSG products are manufactured on three continents ...

Associate, Business Operations

Tustin, CA · On-site

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Coordinate cross-functional input from Business Development, Project Management, Manufacturing ... Two to four years of experience in life sciences, biotechnology, biopharmaceutical services ...

Associate, Business Operations

Tustin, CA · On-site +1

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Coordinate cross-functional input from Business Development, Project Management, Manufacturing ... Two to four years of experience in life sciences, biotechnology, biopharmaceutical services ...

Project Chemistry is a leading cosmetic formulation and innovation lab based in Irvine, California ... Our expertise spans ingredient discovery, biotech-driven IP creation, advanced active system ...

New

Showing results 21-40

Biotechnology Project Manager information

See Riverside, CA salary details

$22

$48

$79

How much do biotechnology project manager jobs pay per hour?

As of Aug 20, 2026, the average hourly pay for biotechnology project manager in Riverside, CA is $48.24, according to ZipRecruiter salary data. Most workers in this role earn between $41.88 and $52.93 per hour, depending on experience, location, and employer.

What does a biotechnology project manager do?

A Biotechnology Project Manager oversees and coordinates projects within the biotechnology industry, ensuring that research and development initiatives, product launches, or clinical trials are completed on time and within budget. They work with cross-functional teams, including scientists, engineers, and regulatory experts, to set project goals, manage resources, and monitor progress. Their responsibilities also include risk management, stakeholder communication, and ensuring compliance with industry regulations. This role is vital for driving innovation and bringing new biotech products or solutions to market efficiently.

What are the key skills and qualifications needed to thrive as a biotechnology project manager, and why are they important?

To thrive as a Biotechnology Project Manager, you need a solid background in biological sciences or engineering, project management expertise, and often an advanced degree such as an MSc or PhD. Familiarity with tools like Microsoft Project, Gantt charts, regulatory compliance systems, and certifications such as PMP are commonly required. Strong leadership, communication, and problem-solving skills set exceptional candidates apart in managing cross-functional teams and complex timelines. These skills and qualities are essential to effectively coordinate scientific projects, ensure regulatory compliance, and deliver successful outcomes in a dynamic biotech environment.

What are some common challenges faced by biotechnology project managers in cross-functional team environments?

Biotechnology Project Managers often work with multidisciplinary teams composed of scientists, regulatory specialists, manufacturing experts, and business development professionals. One common challenge is ensuring clear communication and alignment across these diverse groups, especially when technical jargon or differing priorities create misunderstandings. Additionally, managing project timelines in a highly regulated environment, where unexpected trial results or compliance issues may cause delays, requires strong adaptive planning. Successful Biotechnology Project Managers foster collaboration by setting clear goals, conducting regular check-ins, and proactively addressing potential roadblocks.

What is the difference between Biotechnology Project Manager vs Research Scientist?

AspectBiotechnology Project ManagerResearch Scientist
Required CredentialsBachelor's or Master's in Biotechnology, Project Management certification often preferredMaster's or PhD in Biotechnology or related field
Work EnvironmentProject teams, corporate labs, industry settingsResearch labs, academic institutions, industry research divisions
Employer & Industry UsageBiotech companies, pharmaceutical firms, biotech startupsUniversities, research institutes, biotech companies

The main difference is that a Biotechnology Project Manager oversees project planning, coordination, and execution within biotech companies, focusing on timelines and budgets. In contrast, a Research Scientist conducts experiments and develops new biotech products or knowledge. Both roles require strong biotech credentials, but their daily tasks and focus areas differ significantly.

What are popular job titles related to Biotechnology Project Manager jobs in Riverside, CA?

For Biotechnology Project Manager jobs in Riverside, CA, the most frequently searched job titles are:

What job categories do people searching Biotechnology Project Manager jobs in Riverside, CA look for?

The top searched job categories for Biotechnology Project Manager jobs in Riverside, CA are:

What cities near Riverside, CA are hiring for Biotechnology Project Manager jobs?

Cities near Riverside, CA with the most Biotechnology Project Manager job openings:

Infographic showing various Biotechnology Project Manager job openings in Riverside, CA as of August 2026, with employment types broken down into 86% Full Time, 13% Part Time, and 1% Contract. Highlights an 84% Physical, 2% Hybrid, and 14% Remote job distribution, with an average salary of $100,346 per year, or $48.2 per hour.

R&D Project Manager- Medical Devices

Pyramid Consulting, Inc.

Irvine, CA • On-site

$65 - $70/hr

Other

Medical, Dental, Vision, Retirement

Posted 13 days ago


Job description

Immediate need for a talented R&D Project Manager- Medical Devices. This is a 12+ Months contract opportunity with long-term potential and is located in Irvine California (Hybrid) Please review the job description below and contact me ASAP if you are interested.
Job Diva ID: 26-24192
Pay Range: $65/hr - $70/hour. Employee benefits include, but are not limited to, health insurance (medical, dental, vision), 401(k) plan, and paid sick leave (depending on work location).

Key Responsibilities:

  • Manage one or more large-scale projects/programs, ensuring strict adherence to Quality Systems and Change Control Process.
  • Facilitate the creation and approval of business cases within the program and coordinate the sharing and prioritization of resources among projects.
  • Develop a detailed plan for the program and manage program changes accordingly.
  • Implement program strategies related to quality assurance, risk management, communications, staffing, and other core areas. and communicate program status and data to maintain accurate and current program information for stakeholders.
  • Facilitate core team meetings and other required meetings to support program execution; regularly assess and enhance meeting processes, decision-making, and workflows.
  • Serve as a project and program management subject matter expert, including guiding and mentoring peers.
  • Demonstrate high emotional intelligence; build trust, rapport, and respect with project team members and stakeholders; engage in honest and transparent conversations.
  • Create a culture where teams can act with a high sense of urgency and accountability to meet/exceed individual and project goals.
  • Understand complex problems and drive the team to effective resolution.
  • Display perseverance and maintain appropriate forward momentum by keeping the core team engaged, even when faced with crises and/or changes.
  • Demonstrate strong ability to influence downward, horizontally, and upward.

Key Requirements and Technology Experience:

  • Must have;5+ years of Project/Program Management experience in New Product Development (NPD), leading cross-functional projects from concept through commercialization.
  • Medical Device industry experience with a strong understanding of FDA regulations, ISO 13485, Design Controls, Quality Systems (QMS), and Change Control.
  • Experience managing complex product development involving Software, Firmware, and Hardware (including thermoplastics/disposable medical devices).
  • Proven expertise in project management methodologies and tools, including Agile/Scrum, Jira, Microsoft Project, and/or Azure DevOps, with PMP certification preferred.
  • Strong leadership and stakeholder management skills
  • A minimum of 5 years of direct experience managing New Product Development projects and/or programs of increasing complexity.
  • Demonstrates a record of successfully managing and leading projects in the medical device industry that incorporate a mix of Software, Firmware, and Thermoplastic Hardware and Disposable components.
  • Proficient understanding of Medical Device Regulations and Product Development Process.
  • Demonstrated record of leading within complex organizations require strong management skills.
  • Proven expertise in the usage of MS Office Suite and related project management systems.
  • Ability to see the big picture and determine the course of action from an overall best for the business perspective.
  • Strong analytical skills with the ability to define problems, collect data, establish facts, and draw valid conclusions.
  • Ability to work cooperatively at all levels in a matrix environment to build and maintain the positive relationships required to accomplish organizational goals.
  • Demonstrated proficiency in decision-making, with the capability to negotiate and balance priorities across multiple functional departments. Makes timely decisions in the face of risk and uncertainty.
  • Experience in the medical device industry is highly preferred.
  • Experience in the pharmaceutical, biotechnology, or healthcare sectors may be considered
  • Familiarity with Agile and Scrum methodologies, as well as project management software such as Jira and Microsoft DevOps.
  • Meticulous attention to detail.
  • Ability to lead meetings with external representatives.
  • Adhere to all EHS rules and requirements and take adequate control measures in preventing injuries to themselves and others as well as to the protection of the environment and prevention of pollution under their span of influence/control.
  • Bachelor's Degree in related field (STEM preferred).
  • Master's Degree or equivalent Preferred.
  • PMP/Agile/Scrum Certification Plus.


Our client is a leading Medical Deivces , and we are currently interviewing to fill this and other similar contract positions. If you are interested in this position, please apply online for immediate consideration Pyramid Consulting, Inc. provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, colour, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws. By applying to our jobs, you agree to receive calls, AI-generated calls, text messages, or emails from Pyramid Consulting, Inc. and its affiliates, and contracted partners. Frequency varies for text messages. Message and data rates may apply. Carriers are not liable for delayed or undelivered messages. You can reply STOP to cancel and HELP for help. You can access our privacy policy .